3-Methyladenine-DNA glycosylase (MPG protein) interacts with human RAD23 proteins (Q22254268)

GOA release 2020-03-11

damaged DNA binding

1 reference

GOA release 2020-03-11

F Miao

Miao

1 reference

8 February 2023

M Bouziane

Bouziane

1 reference

8 February 2023

R Dammann

Dammann

1 reference

8 February 2023

C Masutani

Masutani

1 reference

8 February 2023

F Hanaoka

Hanaoka

1 reference

8 February 2023

G Pfeifer

Pfeifer

1 reference

8 February 2023

T R O'Connor

T R

O'Connor

1 reference

Journal of Biological Chemistry

8 February 2023

language of work or name

English

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publication date

15 September 2000

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published in

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volume

275

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issue

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page(s)

28433-8

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cites work

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Mammalian DNA nucleotide excision repair reconstituted with purified protein components.

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DNA repair in eukaryotes

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DNA excision repair pathways

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Interaction of human apurinic endonuclease and DNA polymerase beta in the base excision repair pathway

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Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function

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Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G

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Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome

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Nucleotide excision repair 3' endonuclease XPG stimulates the activity of base excision repairenzyme thymine glycol DNA glycosylase

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XRCC1 polypeptide interacts with DNA polymerase beta and possibly poly (ADP-ribose) polymerase, and DNA ligase III is a novel molecular 'nick-sensor' in vitro

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Involvement of XRCC1 and DNA ligase III gene products in DNA base excision repair.

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XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage

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XRCC1 protein interacts with one of two distinct forms of DNA ligase III

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Mammalian DNA ligases

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A sequence in the N-terminal region of human uracil-DNA glycosylase with homology to XPA interacts with the C-terminal part of the 34-kDa subunit of replication protein A

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Reaction mechanism of human DNA repair excision nuclease

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Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repair

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Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene

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BRCA1 required for transcription-coupled repair of oxidative DNA damage

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Repair of N-methylpurines in specific DNA sequences in Chinese hamster ovary cells: absence of strand specificity in the dihydrofolate reductase gene

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Acrolein genotoxicity in Drosophila melanogaster. I. Somatic and germinal mutagenesis under proficient repair conditions.

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Heterogeneous repair of N-methylpurines at the nucleotide level in normal human cells

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Transcription-coupled repair and human disease

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Expression of the p48 xeroderma pigmentosum gene is p53-dependent and is involved in global genomic repair

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The induction and repair of lesions produced by the photolysis of (6-4) photoproducts in normal and UV-hypersensitive human cells

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Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

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The Saccharomyces cerevisiae DNA repair gene RAD23 encodes a nuclear protein containing a ubiquitin-like domain required for biological function

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Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity

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XPC interacts with both HHR23B and HHR23A in vivo

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Identification and characterization of XPC-binding domain of hHR23B.

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XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes

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Assembly, subunit composition, and footprint of human DNA repair excision nuclease

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HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro

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Identification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination.

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Rad23 links DNA repair to the ubiquitin/proteasome pathway

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Interaction of hHR23 with S5a. The ubiquitin-like domain of hHR23 mediates interaction with S5a subunit of 26 S proteasome

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What Structural Features Determine Repair Enzyme Specificity and Mechanism in Chemically Modified DNA?

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Cloning and characterization of a 3-methyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16

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Human cDNA expressing a functional DNA glycosylase excising 3-methyladenine and 7-methylguanine

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Crystal structure of a human alkylbase-DNA repair enzyme complexed to DNA: mechanisms for nucleotide flipping and base excision

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Purification and characterization of human 3-methyladenine-DNA glycosylase

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Interaction of the recombinant human methylpurine-DNA glycosylase (MPG protein) with oligodeoxyribonucleotides containing either hypoxanthine or abasic sites

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Two enzymes are required from strand incision in repair of alkylated DNA

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Mammalian abasic site base excision repair. Identification of the reaction sequence and rate-determining steps

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Activation of apurinic/apyrimidinic endonuclease in human cells by reactive oxygen species and its correlation with their adaptive response to genotoxicity of free radicals

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A 127 kDa component of a UV-damaged DNA-binding complex, which is defective in some xeroderma pigmentosum group E patients, is homologous to a slime mold protein

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Reconstitution of the DNA base excision-repair pathway

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Base excision repair of oxidative DNA damage activated by XPG protein

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3-Methyladenine and 7-methylguanine exhibit no preferential removal from the transcribed strand of the dihydrofolate reductase gene in Chinese hamster ovary B11 cells

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Identifiers

DOI

10.1074/JBC.M001064200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017